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Journal De Genetique Humaine|March 1, 1980
[Intrafamilial variation in congenital ophthalmoplegia: studies in a Sicilian family]F Mollica, S Li Volti, G Incorpora, et al.Journal De Genetique Humaine|March 1, 1980
Familial partial trisomy: 6q25 leads to 6qterD Duca, M Bene, D Ioan, et al.Journal De Genetique Humaine|March 1, 1980
Peculiar mosaicism 47,XYY/48,XYYY/49,XYYYY in manF Gigliani, P Gabellini, L Marcucci, et al.Journal De Genetique Humaine|March 1, 1980
Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boyJ P Fryns, L Emmery, J Timmermans, et al.Journal De Genetique Humaine|March 1, 1976
The importance of determining the mode of inheritance for the estimation of recurrence risksN Van Regemorter, C SmithJournal De Genetique Humaine|June 1, 1976
[A genealogical study of Steinert's disease (author's transl)]J M Robert, J PernodJournal De Genetique Humaine|September 1, 1984
[Should we expand the indications for analysis of fetal chromosomes?]L Koulischer, Y GillerotJournal De Genetique Humaine|September 1, 1984
[The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years]H Plauchu, C Charrin, J C KossmannJournal De Genetique Humaine|December 1, 1984
[Trisomy 12(pter----q12) and monosomy 21(pter----q21). A propos of a case]M Arnaud, G Bourrouillou, B Sablayrolles, et al.Pageof 47